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. 2025 Mar 7;15(6):411.
doi: 10.3390/nano15060411.

Multilayer Core-Sheath Structured Nickel Wire/Copper Oxide/Cobalt Oxide Composite for Highly Sensitive Non-Enzymatic Glucose Sensor

Affiliations

Multilayer Core-Sheath Structured Nickel Wire/Copper Oxide/Cobalt Oxide Composite for Highly Sensitive Non-Enzymatic Glucose Sensor

Yuxin Wu et al. Nanomaterials (Basel). .

Abstract

The development of micro glucose sensors plays a vital role in the management and monitoring of diabetes, facilitating real-time tracking of blood glucose levels. In this paper, we developed a three-layer core-sheath microwire (NW@CuO@Co3O4) with nickel wire as the core and copper oxide and cobalt oxide nanowires as the sheath. The unique core-sheath structure of microwire enables it to have both good conductivity and excellent electrochemical catalytic activity when used as an electrode for glucose detecting. The non-enzymatic glucose sensor base on a NW@CuO@Co3O4 core-sheath wire exhibits a high sensitivity of 4053.1 μA mM-1 cm-2, a low detection limit 0.89 μM, and a short response time of less than 2 s.

Keywords: cobalt oxide nanowires; copper oxide; core-sheath; nickel wire; non-enzymatic glucose sensor.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
(a) XRD spectrum of the NW@CuO@Co3O4 electrode. XPS spectra of the NW@CuO@Co3O4 electrode, (b) full spectrum, (c) Cu 2p spectrum, (d) Ni 2p spectrum, (e) Co 2p spectrum, and (f) O 1s spectrum.
Figure 2
Figure 2
(a) SEM image of pure nickel wire. (b,c) SEM image of nickel wire after “alloy/de-alloy” treatment. (df) SEM image of NW@CuO@Co3O4 electrode.
Figure 3
Figure 3
(a) TEM image of CuO–Co3O4 composite. (b) TEM image of Co3O4 nanowires, (c,d) TEM images of CuO nanoparticles.
Figure 4
Figure 4
(a) Cyclic voltammograms of pure nickel wire electrode and NW@CuO@Co3O4 electrode at 50 mV s−1 in 0.1 M NaOH solution with and without 1mM glucose added. (b) Cyclic voltammograms of NW@CuO@Co3O4 electrode at 50 mV s−1 in different 0.1M NaOH solutions with different concentrations of glucose added. (c) Cyclic voltammograms of NW@CuO@Co3O4 electrode in 0.1 M NaOH at different scan rates (25~125 mv s−1). (d) Linear fitting diagram of cyclic voltammograms of oxidation peak current and reduction peak current at different scan rates and the half of the scan rate.
Figure 5
Figure 5
Glucose detection performance of NW@CuO@Co3O4 electrode (a) Current versus time curves of adding 0.5 mM glucose six times at 50 s intervals to 0.1 M NaOH solution at different voltages (0.5~0.65 V). (b) Selectivity curve after adding 1 mM glucose, ascorbic acid (AA), dopamine hydrochloride (UA), uric acid (DA), and glucose to 0.1 M NaOH solution in sequence. (c) Amperometric response curve of adding different concentrations of glucose in 0.1 M NaOH solution in sequence at 0.55 V. (d) Linear fitting diagram of current and glucose concentration in alkaline solution.
Figure 6
Figure 6
(a) Stability of NW@CuO@Co3O4 glucose sensors in 0.1 mM glucose solution. (b) EIS curves of NW and NW@CuO@Co3O4. (c) Current responses of five NW@CuO@Co3O4 electrodes in 0.1 M NaOH with 2 mM glucose at 0.55 V.

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